A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602486



Internal ID16389895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32541110..32554748hg38UCSC Ensembl
Innerchr6:32508887..32522525hg19UCSC Ensembl
Innerchr6:32616865..32630503hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3813639
hg1913639
hg1813639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055690
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602486
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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